A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219667



Internal ID20786707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119267875..119515517hg38UCSC Ensembl
chr8:120280115..120527757hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38247643
hg19247643
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425031
Supporting Variants
Samples
Known GenesNOV
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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